Ensures adherence to protocol requirements, protects the rights and
welfare of subjects, assures the integrity of data generated at the site and
directs the conduct of the clinical investigation according to federal and
state regulations and guidance documents.
Required: At least 2 years experience in performing physicals, assessing and treating
patients; strong supervision, interpersonal and communication skills. Must possess exceptional organizational and planning skills and good documentation skills. Must have good conflict resolution skills and be committed to quality and honesty. Must be punctual and have a flexible work schedule.
Preferred: At least 2 years experience in clinical research as an investigator or sub-
Investigator. In-depth knowledge of the clinical research process, including Good Clinical Practices; able to make good, sound decisions
under stress and time constraints.
